DLGAP2 p.Thr29=
c.87G>A · rs982040763 · VCV2658290
Likely benign
Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
very rare (popmax 0.00422%, amr)
Computational evidence
| Protein change | ||
| Missense predictors do not apply to this variant type; conservation carries the signal. | ||
| Splicing | ||
| SpliceAI | — | not assessed · no allele here is in the release |
|---|---|---|
| Constraint at this position | ||
| Conservation | phyloP -1.5 | GERP -3.6 |
| Overall | ||
| CADD | 10.87 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
0.00422%
Admixed American · 1/23,722 alleles
Filtering AF
0.000514%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 0.000192%
Overall
0.000648%
7/1,079,472 alleles · very rare
| Ancestry group | Frequency | 1 in |
|---|---|---|
| Admixed Americangrpmax | 0.00422% | 23,722 |
| African / African-American | 0.0031% | 32,266 |
| Remaining individualsnot grpmax-eligible | 0.00218% | 45,784 |
| European (non-Finnish) | 0.000304% | 329,330 |
Rarity supports pathogenicity (ACMG PM2); frequency above a disease-specific BA1/BS1 threshold argues against it. A variant frequent in one ancestry group can be near-absent in others, so a single global figure can mislead.
Variant & gene context
- Gene
- DLGAP2
- Protein
- p.Thr29=
- Coding
- c.87G>A
- MANE Select
- NM_001346810
- dbSNP
- rs982040763
- Type
- single nucleotide variant
- Location
- chr8:1258864 (GRCh38)
- Gene constraint
- LOEUF 0.425 · pLI 1.00 · ClinGen HI 0/3 (gnomAD)
- Structure
- AlphaFold pLDDT 48.83
Similar variants
- DLGAP2 c.1810+14A>G Benign ★★ same type
- DLGAP2 c.2160+19C>G Benign ★★ same type
- DLGAP2 p.Glu678= Benign ★★ same type
- DLGAP2 p.Pro464Gln Benign ★★ same type
- DLGAP2 c.2203-7G>T Uncertain significance ★ same type
- DLGAP2 p.Ala1019Gly Uncertain significance ★ ⚠ same type
- DLGAP2 p.Ala1026Val Uncertain significance ★ same type
- DLGAP2 p.Ala116Thr Uncertain significance ★ ⚠ same type
Built on 18 open, versioned datasets — ClinVar, gnomAD, AlphaMissense, REVEL, ClinGen & more — plus Sugi Variant's own cross-source analysis. Source data 2026-01–2026-10, ClinVar 2026-10. Full sources & versions →
Cite Sugi Variant
Gür T. Sugi Variant: A Deterministic Per-Variant Germline Reference from a Knowledge Graph for Humans and AI Agents. 2026. doi:10.5281/zenodo.21509445. This variant: https://sugi.bio/variant/dlgap2-p-thr29 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown